Results 71 to 80 of about 11,687 (164)
Transfusion, EarlyView.Abstract Background The increasing diversity of blood donor populations has created new challenges for transfusion services worldwide. The identification of donors lacking relevant high‐prevalence antigens is becoming increasingly important to ensure compatible blood products for alloimmunized patients and to support the development of rare donor ...
Sarah Petermann +7 more
wiley +1 more source
Детские инфекции (Москва)Non-immune hydrops fetalis is a polyetiological disease characterized by high perinatal mortality. The development of non-immune fetal hydrops is associated with diseases of the cardiovascular and lymphatic systems, genetic and chromosomal diseases ...
S. V. Dumova +8 more
doaj +1 more source
Human parvovirus B19 infection and hydrops fetalis in Rio de Janeiro, Brazil
Memorias do Instituto Oswaldo Cruz, 1996 Formalin-fixed paraffin embedded lung and liver tissue from 23 cases of non immune hydrops fetalis and five control cases, in which hydrops were due to syphilis (3) and genetic causes (2), were examined for the presence of human parvovirus B19 by DNA ...
Rita CN Cubel +7 more
doaj +1 more source
Recém-nascido com hidrópsia fetal não imune - experiência de um centro de referência.
Acta Médica Portuguesa, 2008 Nonimmune hydrops fetalis is a rare affection that can result from several disorders. Notwithstanding with the advances in the diagnosis and treatment, its morbidity and mortality are still very high.
Ana Teixeira +3 more
doaj +1 more source
Transfusion, EarlyView.Abstract Background Human parvovirus B19 (B19) is a major pathogen involved in transfusion‐related infections. In Japan, B19 antigen screening is conducted during blood donation, and B19 deoxyribonucleic acid (DNA) levels in pooled plasma have remained below the limit recommended by the U.S. Food and Drug Administration (104 IU/mL).
Yugo Nishiguchi +5 more
wiley +1 more source
Unveiling the elusive: a case of missed hydrops fetalis [PDF]
Hydrops fetalis, characterized by abnormal fluid accumulation in fetal tissues, poses diagnostic challenges often leading to adverse outcomes.
Dange, Shalini +5 more
core +1 more source
Alder–Reilly Anomaly Leading to Incidental Diagnosis of MPS VII in an Asymptomatic Adult
JIMD Reports, Volume 67, Issue 6, November 2026.ABSTRACT Mucopolysaccharidosis type VII (MPS VII; Sly syndrome) is a rare autosomal recessive lysosomal storage disorder caused by deficiency of β‐glucuronidase due to pathogenic variants in the GUSB gene. Impaired degradation of glycosaminoglycans (GAGs) results in multiorgan dysfunction with highly variable clinical presentation, ranging from severe ...
Margaretha G. M. Roemer +5 more
wiley +1 more source
Cerebral Venous Engorgement in Hydrops Fetalis [PDF]
, 2016 A 34-year-old gravida was diagnosed with hydrops fetalis, hydrothorax with cardiac compression, hygroma, ascites, and subcutaneous edema at 20 weeks of gestation..
Qureshi, Adnan I, Kohl, Thomas
core
Recurrent non immune hydrops fetalis: a case report [PDF]
, 2017 Recurrent non-immune fetal hydrops (NIHF) is a known but rare disease. We report a case of recurrent fetal hydrops in a multipara with no significant surgical or medical history.
Varma, Thankam Rana +2 more
core +1 more source
Case report: Giant congenital pulmonary airway malformation initially managed and resected on ECMO
Journal of Pediatric Surgery Case Reports, 2016 Congenital pulmonary airway malformations (CPAM) are a common congenital anomaly, occurring as a result of aberrant formation of pulmonary lobes or segments. Many patients with CPAM are treated with postnatal surgical excision within 1-year of age.
Richard Yeker +3 more
doaj +1 more source